Antibodies directed against the alpha interferon receptor

ABSTRACT

The present invention relates to antibodies against an alpha interferon receptor, as well as to kits comprising such antibodies. The antibodies of the invention are suitable for the assay of the receptors or for their visualization in the case of imaging. The present antibodies and kits can thus be used as diagnostics or imaging agents, or as pharmacological models to test compounds derived from human alpha interferon.

This is a division of Application No. 08/453,090, filed May 30, 1995,which is a continuation of Application No. 07/900,642, filed Jun. 15,1992, now abandoned, which claims priority from PCT/FR90/00758, filedOct. 19, 1990.

The present invention relates to the sequence, in particular to a cDNAsequence, coding for the gene for the alpha interferon receptor.

Interferon is a generic term specifying three antigenic classes: alpha,beta and gamma, of proteins capable of inducing, among other things, anantiviral state and of inhibiting the multiplication of sensitive cells.

Between the alpha and beta interferons, which are produced as aconsequence of viral infection, there exists a sufficiently extensivestructural homology for these two types of interferon to be able toreact via the same cell receptor.

Human alpha interferon is itself a mixture of a dozen proteins with veryextensive homology, encoded by different structural genes. Thesesubtypes have an identical functional spectrum but their specificactivities are different.

Gamma interferon, which is produced by activated lymphocytes, does notpossess any homology with the alpha/beta interferons and it does notreact with their receptor.

At present, the structures of the interferons (which possess about 165amino acids) are quite well known as regards their amino acid sequencesand several studies have been directed towards the analysis of thefunctional domains of these proteins. Hybrid molecules, constructedbetween the interferons of high and low affinity by using restrictionsites on the DNA coding for these interferons, have been used to showthat the N-terminal part of the molecule determines the affinity ofbinding to its cell receptor and, consequently, the specific activity ofthe alpha interferons.

Respiratory diseases of viral origin pose considerable economic problemsfor public health. Clinical trials have shown that alpha interferonprovides 100% protection to volunteers infected with differentrhinoviruses. Similarly, it has been demonstrated that among volunteerstreated with alpha interferon and infected with a coronavirus, 6%develop the symptoms of a cold compared with 37% of the volunteerstreated with placebo.

Nonetheless, although human alpha interferon was found to be efficaciousin these trials, the toxicity that it exerts on the nasal mucosa poses amajor problem.

Interferon also possesses an antitumoral activity in man and at presentit has become the treatment of choice for some cancers. However,interferon injected by the systemic route also exerts toxicity on thenervous system which limits the possibilities of treatment.

In fact, at present, there is no means of determining which interferonshould be used to obtain therapeutic activity and reduced toxicity.Several laboratories have made considerable efforts to constructmodified interferons which might have pronounced activity associatedwith low toxicity. This approach has been shown to be disappointing.

It is now obvious that the possible success of such a project requiresknowledge of the structure of the receptor of the interferons in orderto devise the structure of an agonist. An agonist having a high activityand low toxicity for the nasal mucosa would find a very large market forthe treatment of respiratory diseases of viral origin.

That is why the present invention relates more particularly to theproduction of a protein having the structure of the alpha interferonreceptor and its expression, in particular at the surface of cells, aswell as the DNA sequences coding for the said protein.

Hence, the present invention relates, in the first instance, to thehuman alpha interferon receptor characterized in that it corresponds tothe sequence shown in FIG. 4 or to one of its allelic variants whichdoes not differ from it by more than 3 amino acids.

These allelic variants may include the sequence shown in FIG. 4 in whichthe threonine at position 164 is replaced by an arginine and an asparticacid is inserted between the aspartic acid at position 479 and theglutamic acid at position 480.

The present invention also relates to a DNA sequence coding for thereceptor for human alpha interferon.

This DNA sequence will preferably correspond to the sequence shown inFIG. 4 or to a sequence allelic with the latter.

The structure of the DNA sequence coding for the receptor for humanalpha interferon is analysed in the examples. In particular, it bears asignal peptide. In some cases, it will be possible to delete or replacethis signal peptide by another signal peptide but in most cases it willbe preferable to retain this signal peptide shown in FIG. 4 and hencethe corresponding coding sequence.

This sequence is preferably inserted into a system which ensures itscellular expression in a suitable host cell, in particular at atransmembrane site.

In particular, the present invention relates to the DNA fragment, inparticular the cDNA fragment, characterized in that it codes for thegene of the alpha interferon receptor. In particular, it will correspondto the sequence shown in FIG. 4 or to a sequence allelic with thelatter.

It may thus be the DNA sequence shown in FIG. 4 in which the cytosine atposition 569 is replaced by guanine and a TGA codon inserted between theadenine situated at position 1514 and the thymine at position 1515.

The present invention also relates to non-human cells characterized inthat they express the said receptor for human alpha interferon and to aprocess for the production of the said cells.

According to this process, compatible host cells are transfected orinfected with an element of DNA bearing a DNA sequence coding for thesaid receptor, as well as the elements capable of ensuring theexpression of this sequence in the said cell.

The examples given hereafter demonstrate how it has been possible toexpress this sequence coding for the receptor for human alpha interferon(IFN-alpha h) in non-human mammalian cells, in particular mouse cells.The procedures which make possible the cell expression of exogenous DNAsequences are known. Depending on the host cells, it may be a questionof using self-replicating vectors such as plasmids or integratingvectors, DNA sequences or viral vectors for example. In the case inwhich it is desired to produce a cell line expressing the humanIFN-alpha receptor, the procedure used may be a low yield proceduresince only one line is sought. On the other hand, when the production ofthe protein alone is desired, it is preferable to use vectors ensuringamplification, in particular plasmid vectors comprising an origin ofreplication or multicopy systems of integration.

In addition, the present invention relates to a process for thepreparation of human alpha IFN receptors.

Thus, when it is desired to produce the protein alone, host cellstransformed, transfected or infected by an expression vector for thesaid protein, comprising a DNA sequence coding for the said receptorunder the control of a promoter of transcription of this sequence in thehost as well as the elements ensuring the translation of the protein,will be cultivated in a suitable culture medium and then the proteinobtained will be separated by any appropriate means.

This protein will be used to prepare antibodies, in particularmonoclonal antibodies directed against the receptor; the appropriatetechnology will not be described in detail since it is a knownprocedure.

The invention thus makes it possible to produce:

the receptor for human alpha interferon,

antibodies directed against this receptor, and

cells expressing the said receptor.

The applications of these elements are very varied. First, the receptorin isolation or expressed on the surface of a cell may enable analoguesof human alpha interferon to be tested in order to define the bestagonists.

This type of test may also be performed by means of the correspondingprotein attached to a solid support such as plates, beads, etc. . .These procedures have already been used for other receptors or forantigen-antibody assays.

The receptor agonist assays may be performed by measuring direct bindingor by measuring displacements which make it possible to estimate theaffinity of the agonist in relation to a reference substance, forexample the human alpha IFN.

The antibodies will be used for the assay of the receptors or for theirvisualization in the case of imaging. These are procedures which make itpossible to evaluate certain pathological conditions justifying, forexample, treatment with alpha interferon or which make it possible toevaluate certain conditions in which the level of these receptorsvaries.

Hence, the invention also relates to diagnostic kits containing one ormore of the preceding elements as a diagnostic or imaging agent, or as apharmacological model to test the compounds derived from human alphainterferon.

The receptor protein or the corresponding antibodies may also be used asa pharmacological agent when it is desired to block the human alpha IFNreceptors or when the protein is used as an inhibitor to block humanalpha IFN in certain states in which the over-expression of human alphainterferon may be harmful.

Finally, the antibodies may be used as targetting agent for theinsertion of an active principle coupled to this antibody in thevicinity of a receptor for the human alpha IFN.

The examples and figures given hereafter are non-limiting and will makeit possible to demonstrate other advantages and characteristics of thepresent invention.

BRIEF DESCRIPTION OF THE DRAWINGS

FIGS. 1A and 1B show the binding curves of human alpha interferon B(black symbols) or the hybrid BDBB (white symbols) to the primarytransfectant 10BH7 (FIG. 1A) or to the parental cells BTG 9A (FIG. 1B).

FIGS. 2A and 2B represent the "Southern blot" analysis of the genomicDNA of the primary and secondary transfectants.

FIG. 2A

Well No. 1: EcoRI digestion of the DNA of the primary clone 10BH7hybridized with a Alu probe.

Well No. 2: same DNA hybridized with a Lambda probe.

FIG. 2B

Wells No. 1 and 3: BamHI digestion of the DNA of the two secondarytransfectants 1B4D10 and 2A415 hybridized with a Alu probe.

Well No. 2 and 4: BamHI digestion of the DNA of two negative secondarytransfectants hybridized with a Alu probe.

Well No. 5: BamHI digestion of the DNA of the parental cells BTG 9Ahybridized with a Alu probe.

FIG. 3 shows the "Northern blot" analysis of the RNA polyA⁺ of the twosecondary transfectants (wells No. 1 and 3) and of the parental cells(well No. 2) hybridized with the probe EcoRI 5 kb.

FIGS. 4A-4F show the nucleotide sequence of the cDNA of the receptor forhuman alpha interferon (SEQ ID NO:1) as well as its amino acid sequence(SEQ ID NO:2). The signal peptide and the transmembrane region are shownin boxes. The glycosylation sites linked to nitrogen are underlined bydashes. The two polyadenylation sites and the Sma I restriction site areunderlined.

EXAMPLE 1

Selection of transfected BTG mouse cells sensitive to human alpha Binterferon

Mouse BTG 9A cells are co-transfected with a human cDNA bank cloned in amammalian lambda phage expression vector also containing the bacterialgene neo and the genomic DNA Daudi of high molecular weight in a ratio1:1. This system of co-transfection in which the expression of a humaninterferon receptor may result from the genomic human DNA and/or thehuman cDNA is used to increase the chances of isolating usefultransfectants.

Clones of stable transfectants are selected in a G418 medium at afrequency of 10⁻² -10⁻². In order to detect cell clones sensitive tohuman alpha interferon, transfected clones are treated with 30,000units/ml of human B interferon and infected with VSV. At thisconcentration, mouse BTG cells are insensitive to alpha B interferon buta transfectant clone expressing the receptor gene for human alphainterferon ought to be in an antiviral phase.

In view of the fact that the interferon titer is inversely proportionalto the multiplicity of infection, this viral selection makes it possibleto neutralize the large quantity of VSV produced by the majority of theclones of the unsuitable cells which would abolish the antiviral stateof the clone of the cell of interest. This method implies a rapidabsorption of the virus by the cells followed by a treatment with rabbitanti-VSV antiserum to neutralize the excess of the virus, anddevelopment of the cytopathic effect in a rabbit anti-VSV antiserumcontaining a semi-solid gelose medium. Surviving cellular clones areisolated individually. In order to avoid a chronic VSV infection, thecell clones are subjected to a treatment with mouse alpha/betainterferon and the anti-VSV antiserum is maintained in a G-418 mediumfor one week. They are then retested for their sensitivity to humanalpha B interferon in relation to the VSV or EKC infections. Most ofthese transfected clones are insensitive to human alpha B interferon.Nonetheless, one clone showed an interesting sensitivity to human alphaB interferon. It was then subcloned and designated 10B H7.

The sensitivity of the 10B H7 cells to numerous mouse and human alphainterferons was determined, then the behaviour of these cells wascompared with that of the parental mouse BTG cells.

Table I shows the activity of mouse alpha/beta interferon, human alpha Binterferon, human beta interferon and human gamma interferon tested onmouse parental BTG cells of the transfected 10B H7 clone and of humanWish cells using both the VSV and the EMC viruses.

With respect to mouse interferon, the 10B H7 cells are as sensitive asthe parental BTG cells. Moreover, the 10B H7 cells show a sensitivity atleast 64,000 times greater to human alpha B interferon than the parentalcells. The activity of human beta interferon on the 10B H7 cells is alsoobserved to be increased 8-fold but no antiviral activity of human gammainterferon is detected since it is recognized by a different receptor onboth the parental BTG cells and on the transfected 10B H7 clone. Thespecific antiviral activity of alpha B interferon (4.7×10⁶ units/mg) onthe 10B H7 cells is of the order of the specific activities of the humanalpha interferons on human cells.

                  TABLE I    ______________________________________    Antiviral activities of interferon    preparations tested on:    (units/ml)                                       RATIO           BTG     10BH7     WISH      10BH7/BTG    ______________________________________    Mouse alpha/             12.8 × 10.sup.6                       12,3 × 10.sup.6                                 240     1    beta IFN    Human alpha B             <20       1,27 × 10.sup.6                                 5.4 × 10.sup.6                                         >64,000    IFN    Human beta             200       1,6 × 10.sup.3                                 2,7 × 10.sup.6                                         8    IFN    Human gamma             <1 × 10.sup.3                       <1 × 10.sup.3                                 20 × 10.sup.6                                         --    IFN    ______________________________________

EXAMPLE 2

Transfectants of a mouse BTG cell sensitive to interferon which expressthe receptor for human interferon.

Human alpha B interferon behaves towards 10B H7 cells like alpha Dinterferon on human cells,with similar specific activity and similarapparent binding affinity. Like alpha D interferon on human cells, thebinding of human alpha B interferon to 10B H7 cells may be measured onlyat 37° C.

Several binding experiments were performed with iodinated alpha Binterferon used as probe for the human receptor and a iodinated hybridinterferon designated BDBB which is active on both the parental mouselines and on the clone 10B H7, as positive control. This hybridinterferon which has a specific activity on mouse cells close to that ofhuman alpha B interferon on the 10B H7 cells, could be a probe for themouse and human receptors on both the parental BTG cells and thetransfected 10B H7 cells.

FIGS. 1A and 1B show that the binding of BDBB is similar to the BTG and10B H7 cells. Conversely, the 10B H7 cells bind alpha B interferonspecifically whereas the BTG cells do not. The binding parameterscalculated from the Scatchard data show that the 10B H7 cells expressabout 500 binding sites per cell for alpha B interferon with an apparentKd of 2.10⁻¹⁰ M. This is similar to the values for the BDBB interferon(1,500 binding sites per cell; apparent KD 5.10⁻¹⁰ M), which is activeon both the parental mouse lines and on the clone 10B H7.

In conclusion these results, supplemented with other studies, indicatethat human alpha B interferon binds to a specific receptor on the 10B H7cells but not to the parental mouse cells.

EXAMPLE 3

Cloning of a probe covering the gene for the human alpha interferonreceptor in clones of a secondary transfected cell

Starting from the hypothesis that the 10B H7 cells express a transfectedhuman gene necessary for conferring binding sites and an antiviralactivity of alpha B interferon on a mouse cell, the distribution of thehuman DNA in the transfected 10B H7 genome was investigated.

FIG. 2A is a "Southern blot" with the DNA of the 10B H7 clone usingeither a human Alu sequence which detects human genomic DNA or a probewith lambda DNA in order to detect the integrated cDNA.

Thus it was shown that the transfectants had integrated more than onepart per 1000 of human Daudi DNA and 100 copies of the human cDNA of themammalian library. In view of the considerable amount of human DNA inthis clone, it was necessary to isolate secondary transfectants in orderto clone the DNA sequence responsible for the expression of the receptorin the initial 10B H7 clone. For this purpose, mouse BTG cells wereco-transfected with genomic DNA from the 10B H7 clone and from neopSV2.Cells sensitive to human interferon were isolated. The stable secondarytransfectants were subjected to 4 cycles of treatment with alpha Binterferon and to VSV infection. After subcloning, two independentsecondary clones 1B4D10 and 2A415 were obtained. These two secondaryclones are independent but are derived from the same initial clone. Theyhave the same characteristics as those of the initial clone 10B H7, i.e.sensitivity to human alpha interferon and expression of the receptor attheir surface. These two secondary clones have not retained thesequences associated with the lambda phages in their genome and,consequently, the expression of the receptors for human alpha interferonis due to the genomic DNA of the Daudi cells which had been transfectedinitially into the BTG cells. They have, in fact, conserved the humangenomic sequences. FIG. 2B shows a BamHI digestion of the secondary DNAclones hybridized with a Alu probe which detects the repetitive Alusequences. The two positive secondary clones 1B4D10 and 2A415 have incommon a main band of 18 kb.

A Alu probe was used to screen fragments of size 20-15 kb of a genomiclibrary after complete digestion of the DNA of the secondary clone1B4D10 by BamHI cloned in a lambda phage EMBL 3. The repeated Alusequences containing the BamHI fragment of 18 kb were isolated and thensubcloned in a plasmid vector pUC.

This fragment contains two EcoRI sites giving end fragments of 11 kb and2 kb and a central fragment of 5 kb. There are human Alu repetitivesequences in these three fragments and thus the central 5 kb fragmentmust be deleted from the DNA sequences of the mouse. The central 5 kbEcoRI fragment is present in a EcoRI digestion of the DNA of the twosecondary clones 1B4D10 and 2A415, obtained independently from the sameinitial clone.

EXAMPLE 4

Cloning and nucleotide sequence of the cDNA of the receptor for humanalpha interferon

FIG. 3 shows that the 5 kb EcoRI probe detects a transcript of equalsize in the secondary clones which is absent from the RNA poly A⁺ of theparental BTG cells.

A cDNA library prepared in a lambda ZapII phage vector from the RNA ofthe secondary clone 1B4D10 is screened and the cDNA hybridizing with the5 kb EcoRI probe is isolated. Eight independent cDNA clones, all bearingthe same 3' end, are analysed by sequencing. The longest (1900 bp) haveat their 5' end a HindIII restriction fragment of 400 bp covering onlythe coding sequences and lack the repetitive elements. Used as a probe,this fragment detects the 2.5 kb transcript present in both thesecondary clones and in the Daudi human cells but which is absent fromthe mouse BTG. In view of the fact that point mutations may arise intransfected genes, this HindIII probe of 400 bp has been used to study alambda ZapII cDNA library starting from Daudi human cells in order toisolate complete cDNA clones corresponding to the human transcript.

Overlapping cDNAs isolated from human Daudi cDNA libraries werepreserved in "pBluescript" plasmids starting from the in vivo excisionof ZapII lambda by f1 helper phages. The single-stranded DNA recoveredin the presence of the M13 intermediate phage from bacteria containing"pBluescript" plasmids is sequenced at one end of the cDNA by the chaintermination method (Sanger et al. 1977) and the sequences of the otherend of the cDNA are obtained from the sequence of the double strand inthe plasmid. Oligonucleotides were synthesized and used in particularfor sequencing the DNA when "gaps" appeared in the sequence.

The two strands of the longest cDNAs described in FIGS. 4A-4F werecompletely sequenced.

The sequence of cDNA is of the order of 2784 bp and contains anuntranslated region of 1035 bp at the 3' end which includes twopolyadenylation sequences ATTAAA. The sequence of the open reading frameis complete since it is terminated at the 5' end by a STOP codon. TwoATG codons are found side by side at positions 79 and 82.

In addition to the hydrophobic region of the amino terminus, a secondhydrophobic region (amino acids 456 to 476) was identified. There are 15potential glycosylation sites linked to nitrogen, 12 in the putativeextracellular domain and 3 in the putative intracellular domain.

The molecular weight of the sequence suggested as receptor (includingthe signal peptide) is 63,485 Dalton, and glycosylation may give rise toa value of the order of 95,000-100,000 Dalton for the protein of thenaturally occurring receptor.

The receptor for human alpha interferon appears to be a single protein.Its sequence nonetheless exhibits a certain allelic variation. Suchvariation is found, for example, in the Daudi heterozygbte cells whichexpress two alleles of the receptor, the one corresponding to thesequence described in FIGS. 4A-4F, the other exhibiting a substitutionof a cytosine by a guanine at position 569 and the insertion of threebases T, G and A after the adenine situated at position 1514. At thelevel of the protein, this results in a substitution of the threonine164 by an arginine, and by the insertion of an aspartic acid after theaspartic acid 479.

    __________________________________________________________________________    SEQUENCE LISTING    (1) GENERAL INFORMATION:    (iii) NUMBER OF SEQUENCES: 2    (2) INFORMATION FOR SEQ ID NO:1:    (i) SEQUENCE CHARACTERISTICS:    (A) LENGTH: 2784 base pairs    (B) TYPE: nucleic acid    (C) STRANDEDNESS: single    (D) TOPOLOGY: linear    (ii) MOLECULE TYPE: DNA (genomic)    (xi) SEQUENCE DESCRIPTION: SEQ ID NO:1:    TTAGGACGGGGCGATGGCGGCTGAGAGGAGCTGCGCGTGCGCGAACATGTAACTGGTGGG60    ATCTGCGGCGGCTCCCAGATGATGGTCGTCCTCCTGGGCGCGACGACCCTAGTGCTCGTC120    GCCGTGGGCCCATGGGTGTTGTCCGCAGCCGCAGGTGGAAAAAATCTAAAATCTCCTCAA180    AAAGTAGAGGTCGACATCATAGATGACAACTTTATCCTGAGGTGGAACAGGAGCGATGAG240    TCTGTCGGGAATGTGACTTTTTCATTCGATTATCAAAAAACTGGGATGGATAATTGGATA300    AAATTGTCTGGGTGTCAGAATATTACTAGTACCAAATGCAACTTTTCTTCACTCAAGCTG360    AATGTTTATGAAGAAATTAAATTGCGTATAAGAGCAGAAAAAGAAAACACTTCTTCATGG420    TATGAGGTTGACTCATTTACACCATTTCGCAAAGCTCAGATTGGTCCTCCAGAAGTACAT480    TTAGAAGCTGAAGATAAGGCAATAGTGATACACATCTCTCCTGGAACAAAAGATAGTGTT540    ATGTGGGCTTTGGATGGTTTAAGCTTTACATATAGCTTACTTATCTGGAAAAACTCTTCA600    GGTGTAGAAGAAAGGATTGAAAATATTTATTCCAGACATAAAATTTATAAACTCTCACCA660    GAGACTACTTATTGTCTAAAAGTTAAAGCAGCACTACTTACGTCATGGAAAATTGGTGTC720    TATAGTCCAGTACATTGTATAAAGACCACAGTTGAAAATGAACTACCTCCACCAGAAAAT780    ATAGAAGTCAGTGTCCAAAATCAGAACTATGTTCTTAAATGGGATTATACATATGCAAAC840    ATGACCTTTCAAGTTCAGTGGCTCCACGCCTTTTTAAAAAGGAATCCTGGAAACCATTTG900    TATAAATGGAAACAAATACCTGACTGTGAAAATGTCAAAACTACCCAGTGTGTCTTTCCT960    CAAAACGTTTTCCAAAAAGGAATTTACCTTCTCCGCGTACAAGCATCTGATGGAAATAAC1020    ACATCTTTTTGGTCTGAAGAGATAAAGTTTGATACTGAAATACAAGCTTTCCTACTTCCT1080    CCAGTCTTTAACATTAGATCCCTTAGTGATTCATTCCATATCTATATCGGTGCTCCAAAA1140    CAGTCTGGAAACACGCCTGTGATCCAGGATTATCCACTGATTTATGAAATTATTTTTTGG1200    GAAAACACTTCAAATGCTGAGAGAAAAATTATCGAGAAAAAAACTGATGTTACAGTTCCT1260    AATTTGAAACCACTGACTGTATATTGTGTGAAAGCCAGAGCACACACCATGGATGAAAAG1320    CTGAATAAAAGCAGTGTTTTTAGTGACGCTGTATGTGAGAAAACAAAACCAGGAAATACC1380    TCTAAAATTTGGCTTATAGTTGGAATTTGTATTGCATTATTTGCTCTCCCGTTTGTCATT1440    TATGCTGCGAAAGTCTTCTTGAGATGCATCAATTATGTCTTCTTTCCATCACTTAAACCT1500    TCTTCCAGTATAGATGAGTATTTCTCTGAACAGCCATTGAAGAATCTTCTGCTTTCAACT1560    TCTGAGGAACAAATCGAAAAATGTTTCATAATTGAAAATATAAGCACAATTGCTACAGTA1620    GAAGAAACTAATCAAACTGATGAAGATCATAAAAAATACAGTTCCCAAACTAGCCAAGAT1680    TCAGGAAATTATTCTAATGAAGATGAAAGCGAAAGTAAAACAAGTGAAGAACTACAGCAG1740    GACTTTGTATGACCAGAAATGAACTGTGTCAAGTATAAGGTTTTTCAGCAGGAGTTACAC1800    TGGGAGCCTGAGGTCCTCACCTTCCTCTCAGTAACTACAGAGAGGACGTTTCCTGTTTAG1860    GGAAAGAAAAAACATCTTCAGATCATAGGTCCTAAAAATACGGGCAAGCTCTTAACTATT1920    TAAAAATGAAATTACAGGCCCGGGCACGGTGGCTCACACCTGTAATCCCAGCACTTTGGG1980    AGGCTGAGGCAGGCAGATCATGAGGTCAAGAGATCGAGACCAGCCTGGCCAACGTGGTGA2040    AACCCCATCTCTACTAAAAATACAAAAATTAGCCGGGTAGTAGGTAGGCGCGCGCCTGTT2100    GTCTTAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAAAACAGGAGGTGGAGGTTG2160    CAGTGAGCCGAGATCACGCCACTGCACTCCAGCCTGGTGACAGCGTGAGACTCTTTAAAA2220    AAAGAAATTAAAAGAGTTGAGACAAACGTTTCCTACATTCTTTTCCATGTGTAAAATCAT2280    GAAAAAGCCTGTCACCGGACTTGCATTGGATGAGATGAGTCAGACCAAAACAGTGGCCAC2340    CCGTCTTCCTCCTGTGAGCCTAAGTGCAGCCGTGCTAGCTGCGCACCGTGGCTAAGGATG2400    ACGTCTGTGTTCCTGTCCATCACTGATGCTGCTGGCTACTGCATGTGCCACACCTGTCTG2460    TTCGCCATTCCTAACATTCTGTTTCATTCTTCCTCGGGAGATATTTCAAACATTTGGTCT2520    TTTCTTTTAACACTGAGGGTAGGCCCTTAGGAAATTTATTTAGGAAAGTCTGAACACGTT2580    ATCACTTGGTTTTCTGGAAAGTAGCTTACCCTAGAAAACAGCTGCAAATGCCAGAAAGAT2640    GATCCCTAAAAATGTTGAGGGACTTCTGTTCATTCATCCCGAGAACATTGGCTTCCACAT2700    CACAGTATCTACCCTTACATGGTTTAGGATTAAAGCCAGGCAATCTTTTACTATGAAAAA2760    AAAAAAAAAAAAAAAAAAAAAAAA2784    (2) INFORMATION FOR SEQ ID NO:2:    (i) SEQUENCE CHARACTERISTICS:    (A) LENGTH: 557 amino acids    (B) TYPE: amino acid    (C) STRANDEDNESS: single    (D) TOPOLOGY: linear    (ii) MOLECULE TYPE: protein    (xi) SEQUENCE DESCRIPTION: SEQ ID NO:2:    MetMetValValLeuLeuGlyAlaThrThrLeuValLeuValAlaVal    151015    GlyProTrpValLeuSerAlaAlaAlaGlyGlyLysAsnLeuLysSer    202530    ProGlnLysValGluValAspIleIleAspAspAsnPheIleLeuArg    354045    TrpAsnArgSerAspGluSerValGlyAsnValThrPheSerPheAsp    505560    TyrGlnLysThrGlyMetAspAsnTrpIleLysLeuSerGlyCysGln    65707580    AsnIleThrSerThrLysCysAsnPheSerSerLeuLysLeuAsnVal    859095    TyrGluGluIleLysLeuArgIleArgAlaGluLysGluAsnThrSer    100105110    SerTrpTyrGluValAspSerPheThrProPheArgLysAlaGlnIle    115120125    GlyProProGluValHisLeuGluAlaGluAspLysAlaIleValIle    130135140    HisIleSerProGlyThrLysAspSerValMetTrpAlaLeuAspGly    145150155160    LeuSerPheThrTyrSerLeuLeuIleTrpLysAsnSerSerGlyVal    165170175    GluGluArgIleGluAsnIleTyrSerArgHisLysIleTyrLysLeu    180185190    SerProGluThrThrTyrCysLeuLysValLysAlaAlaLeuLeuThr    195200205    SerTrpLysIleGlyValTyrSerProValHisCysIleLysThrThr    210215220    ValGluAsnGluLeuProProProGluAsnIleGluValSerValGln    225230235240    AsnGlnAsnTyrValLeuLysTrpAspTyrThrTyrAlaAsnMetThr    245250255    PheGlnValGlnTrpLeuHisAlaPheLeuLysArgAsnProGlyAsn    260265270    HisLeuTyrLysTrpLysGlnIleProAspCysGluAsnValLysThr    275280285    ThrGlnCysValPheProGlnAsnValPheGlnLysGlyIleTyrLeu    290295300    LeuArgValGlnAlaSerAspGlyAsnAsnThrSerPheTrpSerGlu    305310315320    GluIleLysPheAspThrGluIleGlnAlaPheLeuLeuProProVal    325330335    PheAsnIleArgSerLeuSerAspSerPheHisIleTyrIleGlyAla    340345350    ProLysGlnSerGlyAsnThrProValIleGlnAspTyrProLeuIle    355360365    TyrGluIleIlePheTrpGluAsnThrSerAsnAlaGluArgLysIle    370375380    IleGluLysLysThrAspValThrValProAsnLeuLysProLeuThr    385390395400    ValTyrCysValLysAlaArgAlaHisThrMetAspGluLysLeuAsn    405410415    LysSerSerValPheSerAspAlaValCysGluLysThrLysProGly    420425430    AsnThrSerLysIleTrpLeuIleValGlyIleCysIleAlaLeuPhe    435440445    AlaLeuProPheValIleTyrAlaAlaLysValPheLeuArgCysIle    450455460    AsnTyrValPhePheProSerLeuLysProSerSerSerIleAspGlu    465470475480    TyrPheSerGluGlnProLeuLysAsnLeuLeuLeuSerThrSerGlu    485490495    GluGlnIleGluLysCysPheIleIleGluAsnIleSerThrIleAla    500505510    ThrValGluGluThrAsnGlnThrAspGluAspHisLysLysTyrSer    515520525    SerGlnThrSerGlnAspSerGlyAsnTyrSerAsnGluAspGluSer    530535540    GluSerLysThrSerGluGluLeuGlnGlnAspPheVal    545550555    __________________________________________________________________________

We claim:
 1. An isolated antibody, wherein said antibody bindsspecifically to a human alpha interferon receptor that comprises thesequence of SEQ ID NO:2.
 2. A kit comprising:(1) at least one antibodyaccording to claim 1, and (2) reagents for an antigen-antibody assay. 3.The kit according to claim 2, wherein said kit further comprises a solidsupport.
 4. The kit according to claim 3, wherein said solid support isa plate or a bead.
 5. An isolated antibody that recognizes a human alphainterferon receptor, wherein said antibody has been raised with animmunogen comprising an isolated recombinant human alpha interferonreceptor comprising the sequence from residues 28-557 of SEQ ID NO:2.